| Disease Browser
|
Parent Node:
 Heart Defects, Congenital (D006330) |
Parent Node:
Holoprosencephaly (D016142) |
Parent Node:
Limb Deformities, Congenital (D017880) |
..Starting node
.. Steinfeld Syndrome (C566655)
|
Child Nodes:
|
Sister Nodes: |
..Aase Smith syndrome (C535332)
|
..Abruzzo Erickson syndrome (C535559)
|
..Acromegaloid facial appearance syndrome (C535655)
|
..Acromicric dysplasia (C535662)  1
|
..Acropectoral syndrome (C535664)
|
..Acropectorovertebral Dysplasia, F-Form (C566319)
|
..Acrorenal syndrome recessive (C535666)
|
..Adams Oliver syndrome (C538225)
|
..Arachnodactyly (D054119) 10
|
..Arms, Malformation of (C566258)
|
..ATELOSTEOGENESIS, TYPE III (OMIM:108721)
|
..B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations (C563745)
|
..Bagatelle Cassidy syndrome (C537796)
|
..Brachydactyly (D059327) 54
|
..Brachymorphism-onychodysplasia-dysphalangism syndrome (C536242)
|
..Brachyolmia, recessive Hobaek type (C537099)
|
..Calabro syndrome (C537960)
|
..Camptobrachydactyly (C537967)
|
..Cartwright Nelson Fryns syndrome (C535917)
|
..Cerebrorenodigital Syndrome with Limb Malformations and Triradiate Acetabula (C563731)
|
..Chondrodysplasia, acromesomelic, with genital anomalies (C537913)
|
..COCOON SYNDROME (OMIM:613630)
|
..Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects (C562515)
|
..Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence (C563127)
|
..Craniomicromelic Syndrome (C566522)
|
..Diaphragmatic Defects, Limb Deficiencies, and Ossification Defects Of Skull (C563380)
|
..Ectrodactyly (C574275)
|
..Ectrodactyly-Polydactyly (C565601)
|
..Ectromelia (D004480) 22
|
..Faciocardiomelic Dysplasia, Lethal (C565578)
|
..Fetal akinesia syndrome, X-linked (C537921)
|
..Foot Deformities, Congenital (D005532) 78
|
..Freire-Maia odontotrichomelic syndrome (C535637)
|
..Fryns syndrome (C538070)
|
..Genee-Wiedemann syndrome (C537680)
|
..Grubben de Cock Borghgraef syndrome (C537621)
|
..Hand and foot deformity with flat facies (C535626)
|
..Hand Deformities, Congenital (D006228) 134
|
..Hanhart syndrome (C535629)
|
..Heart defects limb shortening (C535850)
|
..Hypochondroplasia (C562937)
|
..Hypoglossia-Hypodactylia (C566308)
|
..Ichthyosis tapered fingers midline groove up (C536272)
|
..Kaplan Plauchu Fitch syndrome (C536892)
|
..Kaufman oculocerebrofacial syndrome (C537013)
|
..Krause-Kivlin syndrome (C537617)
|
..Kuster syndrome (C538126)
|
..Laryngeal Atresia, Encephalocele, and Limb Deformities (C564620)
|
..Le Marec Bracq Picaud syndrome (C536997)
|
..Limb Defects, Distal Transverse, with Mental Retardation and Spasticity (C565438)
|
..Limb Deficiencies, Distal, with Micrognathia (C565437)
|
..Limb-mammary syndrome (C535903)
|
..Lower Extremity Deformities, Congenital (D038061) 89
|
..Lynch Lee Murday syndrome (C537713)
|
..Megalodactyly (C562546)
|
..Mental retardation spasticity ectrodactyly (C537446)
|
..Mesomelia-synostoses syndrome (C537348)
|
..Metaphyseal anadysplasia (C537351)
|
..Metaphyseal Anadysplasia 1 (C567545)
|
..Metaphyseal Anadysplasia 2 (C567771)
|
..Microphthalmia with Cyst, Bilateral Facial Clefts, and Limb Anomalies (C564370)
|
..Microphthalmia, Syndromic 6 (C566440)
|
..Multiple Epiphyseal Dysplasia with Robin Phenotype (C563291)
|
..Multiple Pterygium Syndrome, X-Linked (C564072)
|
..Nephrosis deafness urinary tract digital malformation (C536402)
|
..Neu Laxova syndrome (C536405)
|
..Nievergelt syndrome (C536120)
|
..Oculodigitoesophagoduodenal syndrome (C537734)
|
..Palant cleft palate syndrome (C538102)
|
..Penttinen-Aula syndrome (C536653)
|
..Pointer syndrome (C536323)
|
..Polydactyly (D017689) 61
|
..Postaxial Oligodactyly, Tetramelic (C566767)
|
..Powell Chandra Saal syndrome (C538357)
|
..Propping Zerres syndrome (C538052)
|
..Proteus Syndrome (D016715) 1
|
..Radial Ray Deficiency, X-Linked (C564523)
|
..Rapadilino syndrome (C535288)
|
..Reardon Hall Slaney syndrome (C535294)
|
..Renal dysplasia - limb defects syndrome (C537754)
|
..Robinow Syndrome, Autosomal Dominant (C562492)
|
..Robinow syndrome, autosomal recessive (C535863)
|
..Ruzicka Goerz Anton syndrome (C537192)
|
..Short Stature-Obesity Syndrome (C564821)
|
..Splenogonadal fusion limb defects micrognatia (C537318)
|
..Split hand foot deformity (C535777) 2
|
..Split hand foot deformity 1 (C567893)
|
..Split-Hand And Split-Foot With Hypodontia (C566665)
|
..Split-Hand Foot Malformation 2 (C564056) 1
|
..Split-Hand With Obstructive Uropathy, Spina Bifida, And Diaphragmatic Defects (C566662)
|
..Split-Hand/Foot Malformation 4 (C565344)
|
..Split-Hand/Foot Malformation 5 (C564674)
|
..Split-Hand/Foot Malformation 6 (C567616)
|
..Split-hand/foot malformation with long bone deficiency (C536425)
|
..Split-Hand/Foot Malformation With Long Bone Deficiency 2 (C565199)
|
..Split-Hand/Foot Malformation With Long Bone Deficiency 3 (C567245)
|
..Steinfeld Syndrome (C566655)
|
..Stern Lubinsky Durrie syndrome (C537488)
|
..Stratton-Parker Syndrome (C566105)
|
..Syndactyly (D013576) 69
|
..Terminal Osseous Dysplasia and Pigmentary Defects (C564554)
|
..Tetramelic Monodactyly (C566066)
|
..Thanatophoric Dysplasia (D013796) 8
|
..Thoracic Dysplasia-Hydrocephalus Syndrome (C564774)
|
..Thoraco limb dysplasia Rivera type (C536516)
|
..Thoracomelic Dysplasia (C564773)
|
..Ulnar Hypoplasia with Mental Retardation (C564757)
|
..Upper Extremity Deformities, Congenital (D038062) 145
|
..VACTERL association (C536495)
|
..VACTERL association with hydrocephaly, X-linked (C536520)
|
..VACTERL hydrocephaly (C536521)
|
..Viljoen Kallis Voges syndrome (C536349)
|
..Weyers acrofacial dysostosis (C536695)
|
..Wright Dyck syndrome (C536749)
|
..Yunis Varon syndrome (C536719)
|
Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
|
